N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Base Information

Chemical Name:N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide
CAS No.:1028292-44-5
Molecular Formula:C₂₂H₂₇NO₃
Molecular Weight:353.461
Hs Code.:

<i>N</i>-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Synonyms:N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Chemical Property:

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Technology Process of N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

There total 6 articles about N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 118822-54-1
N-(3-hydroxy-4-methoxyphenethyl)-2-phenylacetamide

: 1028292-44-5
N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Guidance literature:: With potassium carbonate; In acetone; for 10h; Heating;
DOI:10.1021/jm020831a

Reference yield:

: 621-59-0
isovanillin

: 1028292-44-5
N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 94 percent / K₂CO₃ / ethanol / 5 h / Heating

2: 88 percent / NH₄OAc; AcOH / 4 h / Heating

3: 63 percent / LiAlH₄ / diethyl ether; tetrahydrofuran / 2 h / Heating

4: 68 percent / 5percent aq. NaOH / CH₂Cl₂ / 2 h / 20 °C

5: 97 percent / conc. HCl / ethanol / 4 h / Heating

6: K₂CO₃ / acetone / 10 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; ammonium acetate; potassium carbonate; acetic acid; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; acetone; 4: Schotten-Baumann reaction;
DOI:10.1021/jm020831a

Reference yield:

: 63909-29-5,55507-05-6
3-benzyloxy-4-methoxy-β-nitrostyrene

: 1028292-44-5
N-{2-[4-methoxy-3-(3-methyl-but-2-enyloxy)-phenyl]-ethyl}-2-phenyl-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 63 percent / LiAlH₄ / diethyl ether; tetrahydrofuran / 2 h / Heating

2: 68 percent / 5percent aq. NaOH / CH₂Cl₂ / 2 h / 20 °C

3: 97 percent / conc. HCl / ethanol / 4 h / Heating

4: K₂CO₃ / acetone / 10 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; acetone; 2: Schotten-Baumann reaction;
DOI:10.1021/jm020831a